ENST00000248633.9:c.957G>C
MANE Select
|
ENSP00000248633.4:p.Gln319His
|
|
ENST00000248633.8:c.957G>C
|
ENSP00000248633.4:p.Gln319His
|
|
ENST00000428214.5:c.957G>C
|
ENSP00000394413.1:p.Gln319His
|
|
ENST00000438045.5:c.274-3591G>C
|
ENSP00000410438.1:n.274-3591G>C
|
|
ENST00000484913.5:n.996G>C
|
|
|
NM_000466.2:c.957G>C
|
NP_000457.1:p.Gln319His
|
|
NM_001282677.1:c.957G>C
|
NP_001269606.1:p.Gln319His
|
|
NM_001282678.1:c.333G>C
|
NP_001269607.1:p.Gln111His
|
|
XR_242246.3:n.1053G>C
|
|
|
XM_017012319.2:c.-710G>C
|
XP_016867808.1:n.-710G>C
|
|
XR_001744808.2:n.67G>C
|
|
|
XR_242246.5:n.1004G>C
|
|
|
NM_000466.3:c.957G>C
MANE Select
|
NP_000457.1:p.Gln319His
|
|
NM_001282677.2:c.957G>C
|
NP_001269606.1:p.Gln319His
|
|
NM_001282678.2:c.333G>C
|
NP_001269607.1:p.Gln111His
|
|